Variant report

Variant	rs13222449
Chromosome Location	chr7:122220781-122220782
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1010498	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10266303	0.98[ASN][1000 genomes]
rs11763594	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12706423	0.96[ASN][1000 genomes]
rs12706424	0.96[ASN][1000 genomes]
rs13222290	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13236662	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17144588	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1990350	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs28514506	0.82[EUR][1000 genomes]
rs28565406	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs28671172	0.83[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs34009656	0.93[ASN][1000 genomes]
rs34208874	0.96[ASN][1000 genomes]
rs35131640	0.96[ASN][1000 genomes]
rs35147547	0.94[ASN][1000 genomes]
rs35345335	0.96[ASN][1000 genomes]
rs35778660	0.96[ASN][1000 genomes]
rs4131663	0.96[ASN][1000 genomes]
rs4521704	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4604372	0.96[ASN][1000 genomes]
rs55913030	0.85[ASN][1000 genomes]
rs6466825	0.96[ASN][1000 genomes]
rs6944494	0.96[ASN][1000 genomes]
rs6952217	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6954625	0.96[ASN][1000 genomes]
rs6956116	0.82[EUR][1000 genomes]
rs6959395	0.96[ASN][1000 genomes]
rs6962479	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6962798	0.93[ASN][1000 genomes]
rs6964649	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7781627	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7782215	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7791524	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7808115	0.96[ASN][1000 genomes]
rs7809699	0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7810271	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017029	chr7:121958574-122338623	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv532178	chr7:122203056-122978846	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122184400-122226000	Weak transcription	Left Ventricle	heart
2	chr7:122198000-122229000	Weak transcription	Fetal Lung	lung
3	chr7:122209200-122221400	Weak transcription	Liver	Liver
4	chr7:122213000-122221200	Weak transcription	Ovary	ovary
5	chr7:122214000-122222600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr7:122214800-122221200	Weak transcription	Gastric	stomach
7	chr7:122215000-122228800	Weak transcription	Adipose Nuclei	Adipose
8	chr7:122217200-122221200	Weak transcription	Pancreas	Pancrea
9	chr7:122217600-122265600	Weak transcription	Aorta	Aorta
10	chr7:122218400-122222800	Weak transcription	HepG2	liver
11	chr7:122219000-122224600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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